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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544911Generated: October 30, 2026

(6-Fluoropyridin-3-yl)boronic acid → HCID 67197126, compound

https://huagongshe.com/reaction/544911

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Fluoropyridin-3-yl)boronic acidHCID 2783397—
ReactantHCID 67199228HCID 67199228—
ProductHCID 67197126HCID 67197126—

Reaction Steps

3-(5-Bromothiophen-2-yl-methyl)-4-methyl-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indole obtained in Example 45-(3) and 6-fluoropyridine-3-boronic acid were treated in a manner similar to Example 45-(4) and 2-(7) to give the titled compound as a colorless powder. APCI-Mass m/Z 485 (M+H). 1H-NMR (DMSO-d6) δ 2.50 (s, 3H), 3.20-3.50 (m, 4H), 3.70 (m, 2H), 4.40 (s, 2H), 4.54 (t, J=5.4 Hz, 1H), 5.09 (d, J=5.3 Hz, 1H), 5.16 (d, J=5.7 Hz, 1H), 5.17 (d, J=5.7 Hz, 1H), 5.36 (d, J=9.0 Hz, 1H), 6.75 (d, J=7.1 Hz, 1H), 6.87 (d, J=3.4 Hz, 1H), 7.00 (t, J=7.7 Hz, 1H), 7.19 (dd, J=8.6, 2.7 Hz, 1H), 7.33 (s, 1H), 7.37 (d, J=8.2 Hz, 1H), 7.44 (d, J=3.4 Hz, 1H), 8.16 (dt, J=8.2, 2.4 Hz, 1H), 8.45 (d, J=2.3 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935674B2
Source datasetuspto-grants-2011_05
ORD IDord-3d922fafacb44a7f9664e27188f9051d
Source noteuspto-grants-2011_05